A novel deep intronic low penetrance RB1 variant in a retinoblastoma family

Retinoblastoma is a malignant retinal tumor of infancy and childhood that arises after biallelic disruption of the RB1 gene on chromosome 13 (1). In heritable retinoblastoma, which often presents b...

[1]  B. Gallie,et al.  Genetics and Molecular Diagnostics in Retinoblastoma—An Update , 2017, Asia-Pacific journal of ophthalmology.

[2]  B. Gallie,et al.  Prenatal versus Postnatal Screening for Familial Retinoblastoma. , 2016, Ophthalmology.

[3]  A. Awan,et al.  Alterations in the RB1 gene in Pakistani patients with retinoblastoma using direct sequencing analysis , 2015, Molecular vision.

[4]  Majida Charif,et al.  Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma , 2011, Molecular vision.

[5]  B. Gallie,et al.  Detection of mosaic RB1 mutations in families with retinoblastoma , 2009, Human mutation.

[6]  M. Subash,et al.  Papilloedema as the sole presenting feature of postpartum cerebral venous sinus thrombosis. , 2009, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.

[7]  Frcsc Prashant Garg National Retinoblastoma Strategy Canadian Guidelines for Care: Stratégie thérapeutique du rétinoblastome guide clinique canadien. , 2009, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.

[8]  L. Orozco,et al.  Spectrum of RB1 gene mutations and loss of heterozygosity in Mexican patients with retinoblastoma: identification of six novel mutations. , 2008, Cancer biomarkers : section A of Disease markers.

[9]  B. Gallie,et al.  Patterns of missplicing caused by RB1 gene mutations in patients with retinoblastoma and association with phenotypic expression , 2008, Human mutation.

[10]  A. Gámez-Pozo,et al.  Pathogenic validation of unique germline intronic variants of RB1 in retinoblastoma patients using minigenes , 2007, Human mutation.

[11]  L. Desjardins,et al.  A deep intronic mutation in the RB1 gene leads to intronic sequence exonisation , 2007, European Journal of Human Genetics.

[12]  J. Alonso,et al.  New RB1 oncogenic mutations and intronic polymorphisms in Serbian retinoblastoma patients: genetic counseling implications , 2006, Journal of Human Genetics.

[13]  B. Gallie,et al.  Spectrum of gross deletions and insertions in the RB1 gene in patients with retinoblastoma and association with phenotypic expression , 2005, Human mutation.

[14]  S. Mittnacht,et al.  A novel constitutional mutation affecting splicing of retinoblastoma tumor suppressor gene intron 23 causes partial loss of pRB activity , 2005, Human mutation.

[15]  B. Gallie,et al.  Retinoblastoma: Revisiting the model prototype of inherited cancer , 2004, American journal of medical genetics. Part C, Seminars in medical genetics.

[16]  B. Horsthemke,et al.  Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma , 1994, Human Genetics.

[17]  D. Frappaz,et al.  A T to C mutation in the polypyrimidine tract of the exon 9 splicing site of the RB1 gene responsible for low penetrance hereditary retinoblastoma , 2002, Journal of medical genetics.